Canonical Allele Identifier: CA354223592

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123010084T>A (hg19) ; chr3:g.123291237T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291237T>A , CM000665.2:g.123291237T>A	GRCh38
NC_000003.11:g.123010084T>A , CM000665.1:g.123010084T>A	GRCh37
NC_000003.10:g.124492774T>A	NCBI36
NG_033882.1:g.162309A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1880A>T	ENSP00000420082.2:p.Glu627Val
ENST00000470367.2:c.2168A>T	ENSP00000514541.1:p.Glu723Val
ENST00000483566.2:c.1880A>T	ENSP00000420252.2:p.Glu627Val
ENST00000699714.1:c.1880A>T	ENSP00000514539.1:p.Glu627Val
ENST00000699715.1:c.1880A>T	ENSP00000514540.1:p.Glu627Val
ENST00000699716.1:c.1880A>T	ENSP00000514542.1:p.Glu627Val
ENST00000699717.1:n.1606A>T
ENST00000699718.1:c.3278A>T	ENSP00000514543.1:p.Glu1093Val
ENST00000462833.6:c.3203A>T MANE Select	ENSP00000419361.1:p.Glu1068Val
ENST00000309879.9:c.2153A>T	ENSP00000308685.5:p.Glu718Val
ENST00000462833.5:c.3203A>T	ENSP00000419361.1:p.Glu1068Val
ENST00000491190.5:c.2177A>T	ENSP00000418537.1:p.Glu726Val
NM_001199642.1:c.2153A>T	NP_001186571.1:p.Glu718Val
NM_183357.2:c.3203A>T	NP_899200.1:p.Glu1068Val
XM_005247077.2:c.3278A>T	XP_005247134.1:p.Glu1093Val
XM_005247078.1:c.2228A>T	XP_005247135.1:p.Glu743Val
XM_006713483.1:c.2177A>T	XP_006713546.1:p.Glu726Val
XM_006713484.1:c.1955A>T	XP_006713547.1:p.Glu652Val
XM_011512359.1:c.2279A>T	XP_011510661.1:p.Glu760Val
XM_011512360.1:c.2189A>T	XP_011510662.1:p.Glu730Val
XM_011512361.1:c.1955A>T	XP_011510663.1:p.Glu652Val
XM_005247077.4:c.3278A>T	XP_005247134.1:p.Glu1093Val
XM_011512359.2:c.2279A>T	XP_011510661.1:p.Glu760Val
XM_011512360.3:c.2189A>T	XP_011510662.1:p.Glu730Val
XM_017005638.1:c.2180A>T	XP_016861127.1:p.Glu727Val
XM_017005639.1:c.2180A>T	XP_016861128.1:p.Glu727Val
NM_001378259.1:c.3278A>T	NP_001365188.1:p.Glu1093Val
NM_183357.3:c.3203A>T MANE Select	NP_899200.1:p.Glu1068Val